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Hereditary renal cell syndromes with genes of mutation
| Syndrome | Gene (chromosome) |
|---|---|
| von Hippel-Lindau | VHL (3p25–26) |
| Hereditary papillary renal carcinoma | C-Met proto-oncogene (7q31–34) |
| Hereditary leiomyomatosis RCC | Fumarate hydratase (1q42–43) |
| Birt–Hogg–Dubé | BHD1 (17p11) |
| Tuberous sclerosis | TSC1 (9q34) or TSC2 (16p13) |
Modified from [5]
